Identification of distinct vascular mural cell populations during zebrafish embryonic development.

hypochord mural cell progenitor pericyte perivascular cells sclerotome vSMC zebrafish

Journal

Developmental dynamics : an official publication of the American Association of Anatomists
ISSN: 1097-0177
Titre abrégé: Dev Dyn
Pays: United States
ID NLM: 9201927

Informations de publication

Date de publication:
19 Dec 2023
Historique:
revised: 14 11 2023
received: 06 04 2023
accepted: 29 11 2023
medline: 19 12 2023
pubmed: 19 12 2023
entrez: 19 12 2023
Statut: aheadofprint

Résumé

Mural cells are an essential perivascular cell population that associate with blood vessels and contribute to vascular stabilization and tone. In the embryonic zebrafish vasculature, pdgfrb and tagln are commonly used as markers for identifying pericytes and vascular smooth muscle cells. However, the overlapping and distinct expression patterns of these markers in tandem have not been fully described. Here, we used the Tg(pdgfrb:Gal4FF; UAS:RFP) and Tg(tagln:NLS-EGFP) transgenic lines to identify single- and double-positive perivascular cell populations on the cranial, axial, and intersegmental vessels between 1 and 5 days postfertilization. From this comparative analysis, we discovered two novel regions of tagln-positive cell populations that have the potential to function as mural cell precursors. Specifically, we found that the hypochord-a reportedly transient structure-contributes to tagln-positive cells along the dorsal aorta. We also identified a unique mural cell progenitor population that resides along the midline between the neural tube and notochord and contributes to intersegmental vessel mural cell coverage. Together, our findings highlight the variability and versatility of tracking both pdgfrb and tagln expression in mural cells of the developing zebrafish embryo and reveal unexpected embryonic cell populations that express pdgfrb and tagln.

Sections du résumé

BACKGROUND BACKGROUND
Mural cells are an essential perivascular cell population that associate with blood vessels and contribute to vascular stabilization and tone. In the embryonic zebrafish vasculature, pdgfrb and tagln are commonly used as markers for identifying pericytes and vascular smooth muscle cells. However, the overlapping and distinct expression patterns of these markers in tandem have not been fully described.
RESULTS RESULTS
Here, we used the Tg(pdgfrb:Gal4FF; UAS:RFP) and Tg(tagln:NLS-EGFP) transgenic lines to identify single- and double-positive perivascular cell populations on the cranial, axial, and intersegmental vessels between 1 and 5 days postfertilization. From this comparative analysis, we discovered two novel regions of tagln-positive cell populations that have the potential to function as mural cell precursors. Specifically, we found that the hypochord-a reportedly transient structure-contributes to tagln-positive cells along the dorsal aorta. We also identified a unique mural cell progenitor population that resides along the midline between the neural tube and notochord and contributes to intersegmental vessel mural cell coverage.
CONCLUSION CONCLUSIONS
Together, our findings highlight the variability and versatility of tracking both pdgfrb and tagln expression in mural cells of the developing zebrafish embryo and reveal unexpected embryonic cell populations that express pdgfrb and tagln.

Identifiants

pubmed: 38112237
doi: 10.1002/dvdy.681
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCATS NIH HHS
ID : UL1TR002345
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM137976
Pays : United States

Informations de copyright

© 2023 American Association for Anatomy.

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Auteurs

Sarah Colijn (S)

Department of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.

Miku Nambara (M)

Department of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.

Gracie Malin (G)

Department of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.

Elena A Sacchetti (EA)

Department of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.

Amber N Stratman (AN)

Department of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.

Classifications MeSH